Use of multiple covariates in assessing treatment-effect modifiers: A methodological review of individual participant data meta-analyses

IF 5 2区 生物学 Q1 MATHEMATICAL & COMPUTATIONAL BIOLOGY Research Synthesis Methods Pub Date : 2023-09-28 DOI:10.1002/jrsm.1674
Peter J. Godolphin, Nadine Marlin, Chantelle Cornett, David J. Fisher, Jayne F. Tierney, Ian R. White, Ewelina Rogozińska
{"title":"Use of multiple covariates in assessing treatment-effect modifiers: A methodological review of individual participant data meta-analyses","authors":"Peter J. Godolphin,&nbsp;Nadine Marlin,&nbsp;Chantelle Cornett,&nbsp;David J. Fisher,&nbsp;Jayne F. Tierney,&nbsp;Ian R. White,&nbsp;Ewelina Rogozińska","doi":"10.1002/jrsm.1674","DOIUrl":null,"url":null,"abstract":"<p>Individual participant data (IPD) meta-analyses of randomised trials are considered a reliable way to assess participant-level treatment effect modifiers but may not make the best use of the available data. Traditionally, effect modifiers are explored one covariate at a time, which gives rise to the possibility that evidence of treatment-covariate interaction may be due to confounding from a different, related covariate. We aimed to evaluate current practice when estimating treatment-covariate interactions in IPD meta-analysis, specifically focusing on involvement of additional covariates in the models. We reviewed 100 IPD meta-analyses of randomised trials, published between 2015 and 2020, that assessed at least one treatment-covariate interaction. We identified four approaches to handling additional covariates: (1) Single interaction model (unadjusted): No additional covariates included (57/100 IPD meta-analyses); (2) Single interaction model (adjusted): Adjustment for the main effect of at least one additional covariate (35/100); (3) Multiple interactions model: Adjustment for at least one two-way interaction between treatment and an additional covariate (3/100); and (4) Three-way interaction model: Three-way interaction formed between treatment, the additional covariate and the potential effect modifier (5/100). IPD is not being utilised to its fullest extent. In an exemplar dataset, we demonstrate how these approaches lead to different conclusions. Researchers should adjust for additional covariates when estimating interactions in IPD meta-analysis providing they adjust their main effects, which is already widely recommended. Further, they should consider whether more complex approaches could provide better information on who might benefit most from treatments, improving patient choice and treatment policy and practice.</p>","PeriodicalId":226,"journal":{"name":"Research Synthesis Methods","volume":"15 1","pages":"107-116"},"PeriodicalIF":5.0000,"publicationDate":"2023-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jrsm.1674","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research Synthesis Methods","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jrsm.1674","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Individual participant data (IPD) meta-analyses of randomised trials are considered a reliable way to assess participant-level treatment effect modifiers but may not make the best use of the available data. Traditionally, effect modifiers are explored one covariate at a time, which gives rise to the possibility that evidence of treatment-covariate interaction may be due to confounding from a different, related covariate. We aimed to evaluate current practice when estimating treatment-covariate interactions in IPD meta-analysis, specifically focusing on involvement of additional covariates in the models. We reviewed 100 IPD meta-analyses of randomised trials, published between 2015 and 2020, that assessed at least one treatment-covariate interaction. We identified four approaches to handling additional covariates: (1) Single interaction model (unadjusted): No additional covariates included (57/100 IPD meta-analyses); (2) Single interaction model (adjusted): Adjustment for the main effect of at least one additional covariate (35/100); (3) Multiple interactions model: Adjustment for at least one two-way interaction between treatment and an additional covariate (3/100); and (4) Three-way interaction model: Three-way interaction formed between treatment, the additional covariate and the potential effect modifier (5/100). IPD is not being utilised to its fullest extent. In an exemplar dataset, we demonstrate how these approaches lead to different conclusions. Researchers should adjust for additional covariates when estimating interactions in IPD meta-analysis providing they adjust their main effects, which is already widely recommended. Further, they should consider whether more complex approaches could provide better information on who might benefit most from treatments, improving patient choice and treatment policy and practice.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
多协变量在评估治疗效果调节剂中的应用:个体参与者数据荟萃分析的方法综述。
随机试验的个体参与者数据(IPD)荟萃分析被认为是评估参与者水平治疗效果调节剂的可靠方法,但可能无法充分利用现有数据。传统上,效应修饰语一次只研究一个协变量,这就产生了治疗协变量相互作用的证据可能是由于来自不同的相关协变量的混淆。我们旨在评估当前在IPD荟萃分析中估计治疗协变量相互作用的做法,特别关注模型中额外协变量的参与。我们回顾了2015年至2020年间发表的100项随机试验的IPD荟萃分析,这些分析评估了至少一种治疗协变量相互作用。我们确定了四种处理额外协变量的方法:(1)单一交互模型(未调整):不包括额外协变量(57/100 IPD荟萃分析);(2) 单一交互作用模型(已调整):对至少一个附加协变量的主要影响进行调整(35/100);(3) 多重相互作用模型:治疗和额外协变量之间至少一种双向相互作用的调整(3/100);(4)三元相互作用模型:治疗、附加协变量和潜在效应修饰因子(5/100)之间形成的三元相互影响。IPD没有得到充分利用。在一个示例数据集中,我们展示了这些方法如何得出不同的结论。研究人员在IPD荟萃分析中估计相互作用时,如果他们调整了主要影响,就应该调整额外的协变量,这已经被广泛推荐。此外,他们应该考虑更复杂的方法是否可以提供更好的信息,说明谁可能从治疗中受益最大,从而改善患者的选择以及治疗政策和实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Research Synthesis Methods
Research Synthesis Methods MATHEMATICAL & COMPUTATIONAL BIOLOGYMULTID-MULTIDISCIPLINARY SCIENCES
CiteScore
16.90
自引率
3.10%
发文量
75
期刊介绍: Research Synthesis Methods is a reputable, peer-reviewed journal that focuses on the development and dissemination of methods for conducting systematic research synthesis. Our aim is to advance the knowledge and application of research synthesis methods across various disciplines. Our journal provides a platform for the exchange of ideas and knowledge related to designing, conducting, analyzing, interpreting, reporting, and applying research synthesis. While research synthesis is commonly practiced in the health and social sciences, our journal also welcomes contributions from other fields to enrich the methodologies employed in research synthesis across scientific disciplines. By bridging different disciplines, we aim to foster collaboration and cross-fertilization of ideas, ultimately enhancing the quality and effectiveness of research synthesis methods. Whether you are a researcher, practitioner, or stakeholder involved in research synthesis, our journal strives to offer valuable insights and practical guidance for your work.
期刊最新文献
Issue Information A tutorial on aggregating evidence from conceptual replication studies using the product Bayes factor Evolving use of the Cochrane Risk of Bias 2 tool in biomedical systematic reviews Exploring methodological approaches used in network meta-analysis of psychological interventions: A scoping review An evaluation of the performance of stopping rules in AI-aided screening for psychological meta-analytical research
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1